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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096195Generated: November 3, 2026

2,6-Lutidine → 3-[(3,4-Dichloro-phenyl)-methoxycarbonylmethyl-amino]-propionic Acid tert-butyl ester

https://huagongshe.com/reaction/1096195

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantMethyl bromoacetateHCID 60984—
Reactant3-(3,4-Dichloro-phenylamino)-propionic Acid tert-butyl esterHCID 66783246—
SolventAcetonitrileHCID 6342—
Product3-[(3,4-Dichloro-phenyl)-methoxycarbonylmethyl-amino]-propionic Acid tert-butyl esterHCID 6678313471.4%

Reaction Conditions

Temperature115 °C

Reaction Steps

A neat solution of 8.82 g (30.39 mmol) of 3-(3,4-dichloro-phenylamino)-propionic acid tert-butyl ester, 13.97 ml (151.97 mmol) of methyl bromoacetate and 17.64 ml (151.97 mmol) of 2,6-lutidine was stirred 14 h at 60° C., diluted with 20 ml of CH3CN and heated at 115° C. for 6 h. The reaction was then partitioned between aq. 10% KHSO4 solution and EtOAc (3×). The organic phases were washed with aq. 10% NaCl solution, dried over Na2SO4 evaporated and purified by flash silica gel column (n-heptane:EtOAc 95:5 to 9:1) to yield 7.86 g (71%) of the title compound as an yellow oil. MS: 362.0 (MH+, 2Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138175B2
Source datasetuspto-grants-2012_03
ORD IDord-626201a9e3994591ab0db9102f675838
Source noteuspto-grants-2012_03